9
Participants
Start Date
November 30, 2013
Primary Completion Date
June 30, 2015
Study Completion Date
June 30, 2015
LCL161
Patients will receive oral LCL161 once a week until unacceptable toxicity, disease progression and/or withdrawal of consent.
Paclitaxel
Patients will receive weekly paclitaxel as intravenous infusion over 1 hour in combination with LCL161, from cycle 2 in dose escalation part or from the first cycle in dose expansion part, and will continue it until unacceptable toxicity, disease progression and/or withdrawal of consent.
Novartis Investigative Site, Nagoya
Novartis Investigative Site, Kobe
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY